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Details

Stereochemistry ABSOLUTE
Molecular Formula C24H24N5O15P3
Molecular Weight 715.3931
Optical Activity UNSPECIFIED
Defined Stereocenters 4 / 4
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of 3'-O-(4-BENZOYL)BENZOYLADENOSINE 5'-TRIPHOSPHATE

SMILES

NC1=C2N=CN([C@@H]3O[C@H](COP(O)(=O)OP(O)(=O)OP(O)(O)=O)[C@@H](OC(=O)C4=CC=C(C=C4)C(=O)C5=CC=CC=C5)[C@H]3O)C2=NC=N1

InChI

InChIKey=AWJJLYZBWRIBCZ-UGTJMOTHSA-N
InChI=1S/C24H24N5O15P3/c25-21-17-22(27-11-26-21)29(12-28-17)23-19(31)20(16(41-23)10-40-46(36,37)44-47(38,39)43-45(33,34)35)42-24(32)15-8-6-14(7-9-15)18(30)13-4-2-1-3-5-13/h1-9,11-12,16,19-20,23,31H,10H2,(H,36,37)(H,38,39)(H2,25,26,27)(H2,33,34,35)/t16-,19-,20-,23-/m1/s1

HIDE SMILES / InChI

Molecular Formula C24H24N5O15P3
Molecular Weight 715.3931
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 4 / 4
E/Z Centers 0
Optical Activity UNSPECIFIED

Approval Year

PubMed

PubMed

TitleDatePubMed
Pharmacological characterization of the human P2Y11 receptor.
1999 Nov
Regulation of phospholipase D by P2X7 receptors in submandibular ductal cells.
2003 Oct
Stimulation of P2X7 receptors elevates Ca2+ and kills retinal ganglion cells.
2005 Jun
P2X(7) receptor blockade prevents ATP excitotoxicity in oligodendrocytes and ameliorates experimental autoimmune encephalomyelitis.
2007 Aug 29
Pharmacological characterization of pannexin-1 currents expressed in mammalian cells.
2009 Feb
Characterization of protoberberine analogs employed as novel human P2X7 receptor antagonists.
2011 Apr 15
Microglial zinc uptake via zinc transporters induces ATP release and the activation of microglia.
2011 Dec
Expression and functional characterization of P2X receptors in mouse alveolar macrophages.
2011 Sep
Purinergic P2X7 receptors mediate cell death in mouse cerebellar astrocytes in culture.
2013 Dec
P2X7 receptors at adult neural progenitor cells of the mouse subventricular zone.
2013 Oct
The azetidine derivative, KHG26792 protects against ATP-induced activation of NFAT and MAPK pathways through P2X7 receptor in microglia.
2015 Dec
Patents
Substance Class Chemical
Created
by admin
on Fri Dec 15 18:11:06 GMT 2023
Edited
by admin
on Fri Dec 15 18:11:06 GMT 2023
Record UNII
4P5DXU1F8Q
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
3'-O-(4-BENZOYL)BENZOYLADENOSINE 5'-TRIPHOSPHATE
Common Name English
ADENOSINE 5'-(TETRAHYDROGEN TRIPHOSPHATE), 3'-(4-BENZOYLBENZOATE)
Systematic Name English
3'-O-(4-BENZOYL)BENZOYL ATP
Common Name English
Code System Code Type Description
EPA CompTox
DTXSID00100222
Created by admin on Fri Dec 15 18:11:06 GMT 2023 , Edited by admin on Fri Dec 15 18:11:06 GMT 2023
PRIMARY
FDA UNII
4P5DXU1F8Q
Created by admin on Fri Dec 15 18:11:06 GMT 2023 , Edited by admin on Fri Dec 15 18:11:06 GMT 2023
PRIMARY
CAS
81790-82-1
Created by admin on Fri Dec 15 18:11:06 GMT 2023 , Edited by admin on Fri Dec 15 18:11:06 GMT 2023
PRIMARY
PUBCHEM
115205
Created by admin on Fri Dec 15 18:11:06 GMT 2023 , Edited by admin on Fri Dec 15 18:11:06 GMT 2023
PRIMARY
MESH
C033901
Created by admin on Fri Dec 15 18:11:06 GMT 2023 , Edited by admin on Fri Dec 15 18:11:06 GMT 2023
PRIMARY